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Synthesis and Interaction of Water Soluble Nucleic Acid Analogs

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Biotechnology and Polymers

Abstract

Water soluble nucleic acid analogs were prepared by grafting uracil, thymine, 5-fluorouracil, hypoxanthine, cytosine, and adenine derivatives containing a hydroxy group onto linear poly (ethyleneimine). These polymers contained about 90 unit% of the nucleic acid bases, and were easily soluble in water at neutral pH resign. The analogs were found to form complementary polymer complexes with each other and with polynucleotides. The interaction study was made on these polymers, and with polynucleotides; poly (uridylic acid) poly (U), poly (adenylic acid) poly (A), poly (inosinic acid) poly (I) and poly (cytidylic acid) poly(C) in water. They were found to form polymer complexes with polynucleotide by specific base-base interaction in aqueous solution.

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© 1991 Springer Science+Business Media New York

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Takemoto, K., Wada, T., Mochizuki, E., Inaki, Y. (1991). Synthesis and Interaction of Water Soluble Nucleic Acid Analogs. In: Gebelein, C.G. (eds) Biotechnology and Polymers. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-3844-8_3

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  • DOI: https://doi.org/10.1007/978-1-4615-3844-8_3

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4613-6715-4

  • Online ISBN: 978-1-4615-3844-8

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